Inherited lipid storage diseases of the central nervous system.
Percy, A K
Inherited lipid storage diseases of the central nervous system. [electronic resource] - Current problems in pediatrics Sep 1979 - 1-51 p. digital
Publication Type: Journal Article; Review
0045-9380
10.1016/s0045-9380(79)80020-1 doi
Adolescent
Adult
Central Nervous System Diseases--diagnosis
Child
Child, Preschool
Fabry Disease--diagnosis
Female
Gangliosidoses--diagnosis
Gaucher Disease--diagnosis
Humans
Infant
Infant, Newborn
Leukodystrophy, Globoid Cell--diagnosis
Leukodystrophy, Metachromatic--diagnosis
Lipid Metabolism, Inborn Errors--diagnosis
Male
Middle Aged
Mucolipidoses--diagnosis
Niemann-Pick Diseases--diagnosis
Sandhoff Disease--diagnosis
Sphingolipidoses--diagnosis
Sphingolipids--metabolism
Tay-Sachs Disease--diagnosis
Inherited lipid storage diseases of the central nervous system. [electronic resource] - Current problems in pediatrics Sep 1979 - 1-51 p. digital
Publication Type: Journal Article; Review
0045-9380
10.1016/s0045-9380(79)80020-1 doi
Adolescent
Adult
Central Nervous System Diseases--diagnosis
Child
Child, Preschool
Fabry Disease--diagnosis
Female
Gangliosidoses--diagnosis
Gaucher Disease--diagnosis
Humans
Infant
Infant, Newborn
Leukodystrophy, Globoid Cell--diagnosis
Leukodystrophy, Metachromatic--diagnosis
Lipid Metabolism, Inborn Errors--diagnosis
Male
Middle Aged
Mucolipidoses--diagnosis
Niemann-Pick Diseases--diagnosis
Sandhoff Disease--diagnosis
Sphingolipidoses--diagnosis
Sphingolipids--metabolism
Tay-Sachs Disease--diagnosis